When phenyl 3,4-dimethylbenzoate undergoes electrophilic aromatic substitution, one ring reacts much more readily than t

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When phenyl 3,4-dimethylbenzoate undergoes electrophilic aromatic substitution, one ring reacts much more readily than t

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When Phenyl 3 4 Dimethylbenzoate Undergoes Electrophilic Aromatic Substitution One Ring Reacts Much More Readily Than T 1
When Phenyl 3 4 Dimethylbenzoate Undergoes Electrophilic Aromatic Substitution One Ring Reacts Much More Readily Than T 1 (23.43 KiB) Viewed 93 times
When phenyl 3,4-dimethylbenzoate undergoes electrophilic aromatic substitution, one ring reacts much more readily than the other. (a) Which one is it? Encircle the ring (b) Explain your answer. (c) Draw the resulting product/s when it undergoes bromination reaction. (10 pts)
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